ID

13407

Description

Phase 1 clinical trial for intrasurgical hyperthermic intraperitoneal chemoperfusion with cisplatin (HIPEC) in patients with ovarian cancer recidiv EudraCT Nr.: 2010-024352-28 Principal investigator und authorized representative of Sponsor: PD Dr. med. Oliver Zivanovic Center for Obstetrics and Gynaecology University Hospital Bonn Sigmund-Freud-Str. 25 53105 Bonn Sponsor: Rheinische Friedrich-Wilhelms-Universität Bonn represented by the Dean of Medical Faculty

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  1. 2016-02-11 2016-02-11 -
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11 februari 2016

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Visit 2 Phase 1 clinical trial for intrasurgical hyperthermic intraperitoneal chemoperfusion with cisplatin (HIPEC) in patients with ovarian cancer recidiv

Anglais

Case report form (HIPEC) Visit 2

1 Formulaires  
Patient Identification
Description

Patient Identification

Patient number
Description

Patient number

Type de données

integer

Alias
UMLS CUI [1]
C1830427
CRF number
Description

CRF number

Type de données

integer

Alias
UMLS CUI [1,1]
C1516308
UMLS CUI [1,2]
C0449788
Date of visit
Description

Date

Type de données

date

Alias
UMLS CUI [1]
C0011008
Debulking surgery
Description

Debulking surgery

Date of surgery
Description

Surgery date

Type de données

date

Alias
UMLS CUI [1]
C0011008
Please give the time the surgery procedure started
Description

Surgery Start time

Type de données

time

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C2114713
Please give the time the surgical procedure was completed
Description

Surgery end time

Type de données

time

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C2711097
Time from incision to suture
Description

Time from incision to suture

Type de données

float

Unités de mesure
  • Minutes
Alias
UMLS CUI [1,1]
C2116297
UMLS CUI [1,2]
C0009068
Minutes
Type of surgery:Hysterectomy
Description

Hysterectomy

Type de données

boolean

Alias
UMLS CUI [1]
C0020699
Type of surgery:unilateral salpingo-oophorectomy
Description

Salpingo-oophorectomy

Type de données

boolean

Alias
UMLS CUI [1]
C0041692
Type of surgery:bilateral salpingectomy with oophorectomy
Description

Salpingo-oophorectomy

Type de données

boolean

Alias
UMLS CUI [1]
C0195495
Type of surgery: Right hemicolectomy
Description

Right hemicolectomy

Type de données

boolean

Alias
UMLS CUI [1]
C0192861
Type of surgery:Transverse colectomy
Description

Transverse colectomy

Type de données

boolean

Alias
UMLS CUI [1]
C0192863
Type of surgery: left colectomy
Description

Left colectomy

Type de données

boolean

Alias
UMLS CUI [1]
C0192865
Type of surgery: Stripping of pelvic peritoneum
Description

Stripping of pelvic peritoneum

Type de données

boolean

Alias
UMLS CUI [1,1]
C0230295
UMLS CUI [1,2]
C0185047
Type of surgery: Excision of periaortic lymph nodes
Description

Excision of periaortic lymph nodes

Type de données

boolean

Alias
UMLS CUI [1]
C0193874
Type of surgery: Appendectomy
Description

Appendectomy

Type de données

boolean

Alias
UMLS CUI [1]
C0003611
Type of surgery:Splenectomy
Description

Splenectomy

Type de données

boolean

Alias
UMLS CUI [1]
C0037995
Type of surgery: Rectosigmoidectomy
Description

Rectosigmoidectomy

Type de données

boolean

Alias
UMLS CUI [1]
C0193063
Type of surgery: Colostomy Procedure
Description

Colostomy

Type de données

boolean

Alias
UMLS CUI [1]
C0009410
Type of surgery: Resection of small intestines
Description

Resection of small intestines

Type de données

boolean

Alias
UMLS CUI [1]
C0192571
Type of surgery: Diaphragm stripping
Description

Diaphragm stripping

Type de données

boolean

Alias
UMLS CUI [1,1]
C0198438
UMLS CUI [1,2]
C0185047
Type of surgery: supracolic omentectomy
Description

Omentectomy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0198614
UMLS CUI [1,2]
C0446612
Type of surgery:infracolic omentectomy
Description

Omentectomy

Type de données

boolean

Alias
UMLS CUI [1]
C0456314
Type of surgery:Complete pelvic lymph node excision
Description

Pelvic lymph node excision

Type de données

boolean

Alias
UMLS CUI [1]
C0398429
Type of surgery:Sampling of lymph node
Description

Lymph node sampling

Type de données

boolean

Alias
UMLS CUI [1]
C0398417
Please specifiy any other type of surgery performed
Description

Other surgery

Type de données

text

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C0543467
Was there a residue after surgery?
Description

Residual tumor

Type de données

text

Alias
UMLS CUI [1]
C0543478
Outcome of surgery and HIPEC
Description

Surgery outcome

Type de données

text

Alias
UMLS CUI [1]
C0184788
Please specify any complications during surgery and HIPEC such as: i.e adhesions
Description

Surgery outcome

Type de données

text

Alias
UMLS CUI [1]
C0184788
Biopsy sample of tumor tissue collected (separate consent required)
Description

Tumor biopsy

Type de données

boolean

Alias
UMLS CUI [1]
C0677862
HIPEC
Description

HIPEC

Has the HIPEC Procedure been performed? If "No", please specify the reason why below.
Description

Procedure performed

Type de données

boolean

Alias
UMLS CUI [1,1]
C0184661
UMLS CUI [1,2]
C0884358
Please specify the reason why the HIPEC-Procedure has not been performed
Description

Procedure not performed

Type de données

text

Alias
UMLS CUI [1,1]
C0184661
UMLS CUI [1,2]
C0445106
Date the HIPEC-Procedure has been performed
Description

Procedure date

Type de données

date

Alias
UMLS CUI [1,1]
C0184661
UMLS CUI [1,2]
C0011008
Time procedure was started
Description

Procedure Start time

Type de données

time

Alias
UMLS CUI [1,1]
C0184661
UMLS CUI [1,2]
C1301880
Time procedure was completed
Description

Procedure end time

Type de données

time

Alias
UMLS CUI [1,1]
C0184661
UMLS CUI [1,2]
C1522314
Used dose in planned escalation scheme
Description

Dose escalation

Type de données

text

Alias
UMLS CUI [1]
C3816728
Total dose applied (calculated from dose in mg multiplicated with body surface in square meter)
Description

Dose escalation

Type de données

integer

Unités de mesure
  • mg
Alias
UMLS CUI [1]
C3816728
mg
Was there a reaction during application? If "yes", please fill in AE form
Description

Reaction

Type de données

boolean

Alias
UMLS CUI [1]
C0443286
Please give the total volume applied during perfusion
Description

Total volume applied

Type de données

integer

Unités de mesure
  • ml
Alias
UMLS CUI [1]
C2826310
ml
Please specify any particularities occurred during HIPEC Procedure
Description

Comments

Type de données

text

Alias
UMLS CUI [1]
C0947611
Pharmacokinetics
Description

Pharmacokinetics

Blood sampling to validate concentration of cisplatin (ng/ml)
Description

Blood sampling

Type de données

boolean

Alias
UMLS CUI [1]
C0005834
Measuring point (from start of perfusion)
Description

Measuring point

Type de données

text

Alias
UMLS CUI [1,1]
C0242485
UMLS CUI [1,2]
C1442880
Measuring point valid?
Description

Measuring point

Type de données

boolean

Alias
UMLS CUI [1,1]
C0242485
UMLS CUI [1,2]
C1442880
Concentration of Cisplatin
Description

Concentration of Cisplatin

Type de données

text

Unités de mesure
  • ng/ml
Alias
UMLS CUI [1]
C0365714
ng/ml
Comments on any particularities during blood sampling and testing. Please specify measuring point
Description

Comments

Type de données

text

Alias
UMLS CUI [1]
C0947611
Sample of perfusate taken?
Description

Sample of perfusate

Type de données

boolean

Alias
UMLS CUI [1,1]
C0200345
UMLS CUI [1,2]
C0029704
Measuring point (from start of perfusion)
Description

Measuring point

Type de données

text

Alias
UMLS CUI [1,1]
C0242485
UMLS CUI [1,2]
C1442880
Measuring point valid?
Description

Measuring point

Type de données

boolean

Alias
UMLS CUI [1,1]
C0242485
UMLS CUI [1,2]
C1442880
Concentration of Cisplatin
Description

Concentration of Cisplatin

Type de données

text

Unités de mesure
  • ng/ml
Alias
UMLS CUI [1]
C0365714
ng/ml
Comments on any particularities during perfusate sampling and testing. Please specify measuring point
Description

Comments

Type de données

text

Alias
UMLS CUI [1]
C0947611
Recording of CTCAE: Have any AE occurred perioperative or since the last Visit? If "Yes" please fill in AE-Form
Description

CTCAE

Type de données

boolean

Alias
UMLS CUI [1]
C1516728
Has concomitant medication been subject to change? If "Yes" please fill in Concomitant medication form.
Description

Concomitant agent

Type de données

boolean

Alias
UMLS CUI [1]
C2347852
Confirmation of correctness
Description

Confirmation of correctness

Confirmatin of investigator: I hereby confirm that I personally checked this CRF for completeness and correctness. All data and statements in this CRF are ,according to best knowlwdge ,complete and correct.
Description

Confirmation

Type de données

boolean

Alias
UMLS CUI [1]
C0750484
Name of Investigator
Description

Name of Investigator

Type de données

text

Alias
UMLS CUI [1]
C2826892
Signature of investigator
Description

Signature

Type de données

text

Alias
UMLS CUI [1]
C1519316
Date of completion of this form
Description

Date of completion

Type de données

date

Alias
UMLS CUI [1]
C0011008
Retour au début de la page

Similar models

Case report form (HIPEC) Visit 2

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Patient Identification
Patient number
Item
Patient number
integer
C1830427 (UMLS CUI [1])
CRF number
Item
CRF number
integer
C1516308 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Date
Item
Date of visit
date
C0011008 (UMLS CUI [1])
Item Group
Debulking surgery
Surgery date
Item
Date of surgery
date
C0011008 (UMLS CUI [1])
Surgery Start time
Item
Please give the time the surgery procedure started
time
C0543467 (UMLS CUI [1,1])
C2114713 (UMLS CUI [1,2])
Surgery end time
Item
Please give the time the surgical procedure was completed
time
C0543467 (UMLS CUI [1,1])
C2711097 (UMLS CUI [1,2])
Time from incision to suture
Item
Time from incision to suture
float
C2116297 (UMLS CUI [1,1])
C0009068 (UMLS CUI [1,2])
Hysterectomy
Item
Type of surgery:Hysterectomy
boolean
C0020699 (UMLS CUI [1])
Salpingo-oophorectomy
Item
Type of surgery:unilateral salpingo-oophorectomy
boolean
C0041692 (UMLS CUI [1])
Salpingo-oophorectomy
Item
Type of surgery:bilateral salpingectomy with oophorectomy
boolean
C0195495 (UMLS CUI [1])
Right hemicolectomy
Item
Type of surgery: Right hemicolectomy
boolean
C0192861 (UMLS CUI [1])
Transverse colectomy
Item
Type of surgery:Transverse colectomy
boolean
C0192863 (UMLS CUI [1])
Left colectomy
Item
Type of surgery: left colectomy
boolean
C0192865 (UMLS CUI [1])
Stripping of pelvic peritoneum
Item
Type of surgery: Stripping of pelvic peritoneum
boolean
C0230295 (UMLS CUI [1,1])
C0185047 (UMLS CUI [1,2])
Excision of periaortic lymph nodes
Item
Type of surgery: Excision of periaortic lymph nodes
boolean
C0193874 (UMLS CUI [1])
Appendectomy
Item
Type of surgery: Appendectomy
boolean
C0003611 (UMLS CUI [1])
Splenectomy
Item
Type of surgery:Splenectomy
boolean
C0037995 (UMLS CUI [1])
Rectosigmoidectomy
Item
Type of surgery: Rectosigmoidectomy
boolean
C0193063 (UMLS CUI [1])
Colostomy
Item
Type of surgery: Colostomy Procedure
boolean
C0009410 (UMLS CUI [1])
Resection of small intestines
Item
Type of surgery: Resection of small intestines
boolean
C0192571 (UMLS CUI [1])
Diaphragm stripping
Item
Type of surgery: Diaphragm stripping
boolean
C0198438 (UMLS CUI [1,1])
C0185047 (UMLS CUI [1,2])
Omentectomy
Item
Type of surgery: supracolic omentectomy
boolean
C0198614 (UMLS CUI [1,1])
C0446612 (UMLS CUI [1,2])
Omentectomy
Item
Type of surgery:infracolic omentectomy
boolean
C0456314 (UMLS CUI [1])
Pelvic lymph node excision
Item
Type of surgery:Complete pelvic lymph node excision
boolean
C0398429 (UMLS CUI [1])
Lymph node sampling
Item
Type of surgery:Sampling of lymph node
boolean
C0398417 (UMLS CUI [1])
Other surgery
Item
Please specifiy any other type of surgery performed
text
C0205394 (UMLS CUI [1,1])
C0543467 (UMLS CUI [1,2])
Item
Was there a residue after surgery?
text
C0543478 (UMLS CUI [1])
Residual tumor
Code List
Was there a residue after surgery?
CL Item
makroscopic no residue (0)
CL Item
<1cm residual tumor  (1)
CL Item
≥1cm residual tumor (2)
Item
Outcome of surgery and HIPEC
text
C0184788 (UMLS CUI [1])
Surgery outcome
Code List
Outcome of surgery and HIPEC
CL Item
without complications (1)
CL Item
with complications (Please fill in AE-Form and specify complications below) (2)
Surgery outcome
Item
Please specify any complications during surgery and HIPEC such as: i.e adhesions
text
C0184788 (UMLS CUI [1])
Tumor biopsy
Item
Biopsy sample of tumor tissue collected (separate consent required)
boolean
C0677862 (UMLS CUI [1])
Item Group
HIPEC
Procedure performed
Item
Has the HIPEC Procedure been performed? If "No", please specify the reason why below.
boolean
C0184661 (UMLS CUI [1,1])
C0884358 (UMLS CUI [1,2])
Procedure not performed
Item
Please specify the reason why the HIPEC-Procedure has not been performed
text
C0184661 (UMLS CUI [1,1])
C0445106 (UMLS CUI [1,2])
Procedure date
Item
Date the HIPEC-Procedure has been performed
date
C0184661 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Procedure Start time
Item
Time procedure was started
time
C0184661 (UMLS CUI [1,1])
C1301880 (UMLS CUI [1,2])
Procedure end time
Item
Time procedure was completed
time
C0184661 (UMLS CUI [1,1])
C1522314 (UMLS CUI [1,2])
Item
Used dose in planned escalation scheme
text
C3816728 (UMLS CUI [1])
Dose escalation
Code List
Used dose in planned escalation scheme
CL Item
I/I 60mg/sqm (1)
CL Item
II/II 80mg/sqm (2)
CL Item
III/III 100mg/sqm (3)
Dose escalation
Item
Total dose applied (calculated from dose in mg multiplicated with body surface in square meter)
integer
C3816728 (UMLS CUI [1])
Reaction
Item
Was there a reaction during application? If "yes", please fill in AE form
boolean
C0443286 (UMLS CUI [1])
Total volume applied
Item
Please give the total volume applied during perfusion
integer
C2826310 (UMLS CUI [1])
Comments
Item
Please specify any particularities occurred during HIPEC Procedure
text
C0947611 (UMLS CUI [1])
Item Group
Pharmacokinetics
Blood sampling
Item
Blood sampling to validate concentration of cisplatin (ng/ml)
boolean
C0005834 (UMLS CUI [1])
Item
Measuring point (from start of perfusion)
text
C0242485 (UMLS CUI [1,1])
C1442880 (UMLS CUI [1,2])
Measuring point
Code List
Measuring point (from start of perfusion)
CL Item
0min (before application of chemo) (1)
CL Item
15min (2)
CL Item
30min (3)
CL Item
45min (4)
CL Item
60min (5)
CL Item
75min (6)
CL Item
90min (7)
CL Item
3h (8)
CL Item
6h (9)
CL Item
12h (10)
CL Item
18h (11)
CL Item
24h (12)
Measuring point
Item
Measuring point valid?
boolean
C0242485 (UMLS CUI [1,1])
C1442880 (UMLS CUI [1,2])
Concentration of Cisplatin
Item
Concentration of Cisplatin
text
C0365714 (UMLS CUI [1])
Comments
Item
Comments on any particularities during blood sampling and testing. Please specify measuring point
text
C0947611 (UMLS CUI [1])
Sample of perfusate
Item
Sample of perfusate taken?
boolean
C0200345 (UMLS CUI [1,1])
C0029704 (UMLS CUI [1,2])
Item
Measuring point (from start of perfusion)
text
C0242485 (UMLS CUI [1,1])
C1442880 (UMLS CUI [1,2])
Measuring point
Code List
Measuring point (from start of perfusion)
CL Item
0min (before application of chemo) (1)
CL Item
15min (2)
CL Item
30min (3)
CL Item
45min (4)
CL Item
60min (5)
CL Item
75min (6)
CL Item
90min (7)
Measuring point
Item
Measuring point valid?
boolean
C0242485 (UMLS CUI [1,1])
C1442880 (UMLS CUI [1,2])
Concentration of Cisplatin
Item
Concentration of Cisplatin
text
C0365714 (UMLS CUI [1])
Comments
Item
Comments on any particularities during perfusate sampling and testing. Please specify measuring point
text
C0947611 (UMLS CUI [1])
CTCAE
Item
Recording of CTCAE: Have any AE occurred perioperative or since the last Visit? If "Yes" please fill in AE-Form
boolean
C1516728 (UMLS CUI [1])
Concomitant agent
Item
Has concomitant medication been subject to change? If "Yes" please fill in Concomitant medication form.
boolean
C2347852 (UMLS CUI [1])
Item Group
Confirmation of correctness
Confirmation
Item
Confirmatin of investigator: I hereby confirm that I personally checked this CRF for completeness and correctness. All data and statements in this CRF are ,according to best knowlwdge ,complete and correct.
boolean
C0750484 (UMLS CUI [1])
Name of Investigator
Item
Name of Investigator
text
C2826892 (UMLS CUI [1])
Signature
Item
Signature of investigator
text
C1519316 (UMLS CUI [1])
Date of completion
Item
Date of completion of this form
date
C0011008 (UMLS CUI [1])
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